lung cancer the new staging system · 5th edition Тnm classification (lung cancer) -1997 6th...
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LUNG CANCERthe new Staging
System
G.KIROVA
TOKUDA HOSPITAL SOFIA
STAGING SYSTEM
• Provides standardized nomenclature for exchanging information
• Groups patients according to the biologic behavior of their tumors
• Aids stratification of patients on the basis of different treatment strategies
• Enables evaluation of treatment strategies
• Defines patients prognosis
MAIN CHANGES7th Edition
9 new classifications
6 main changes
Мх elimination
Parallel anatomic and prognostic staging
Melanoma
GI carcinoma
GIST
Appendix carcinoma
Neuroendocrine tumors:
stomach, bowels, appendix,
lung
Intrahepatic
cholangiocarcinoma
Merkel cell carcinoma
Sarcoma uteri
Suprarenal cancer9ne
w c
lass
ific
atio
ns
6“b
ig”
Esophagus
Stomach
Lung
Skin
Cervix
Prostate
MAIN CHANGES7th Edition
Elimination of category Мх сМх could not exist (could not be proved)
рМх does not exist
рМ0 does not exist (except after autopsy)
сМ0 = clinically without metastasis; cM0 instead pM0 in case of
negative biopsy result from an existing lesion
сМ1 = clinically proved metastasis
рМ1 = pathologically proved metastasis (p.ex. cut biopsy)
MAIN CHANGES7th Edition
6“b
ig”
Esophagus
Stomach
Lung Skin
Cervix
Prostate
MAIN CHANGES7th Edition
TREATMENT POLICY
• Primary methods of lung cancer staging
– Clinical (non-invasive and minimally invasive)
– Pathological
• Clinical vs pathological staging (level of agreement 35% vs55%)
• Lung resection as the only curative treatment for lung cancer
• The goal of the preoperative evaluation is to not precludepatients from attempting surgical resection
• Pathological staging as a reference standard
Lopez-Encuentra et al; Comparison between clinical and pathological staging in 2994 cases of lung cancer; Ann Thor Surg 2005;79:974-979
Clifton F. Mountain
1924 - 2007
2nd, 3rd and 4th Editions of TNM classifiation (lung cancer) -1973 -1987
American Join Committee on Cancer
Union Internationale Contre le Cancer
2155 cases; MD Anderson Cancer Center; Texas
І stage
ІІ stage
ІІІ А stage
ІІІ Б stage
ІV stage
Т 1-2 N 0 М0
Т 1-2 N 1 М0
Т 1-3 N 2 М0
Т 3 N 0-1 M0
any Т N 3 M0
Т 4 any N М0
any Т any N М1
4th Edition ТNM classification (lung cancer) -1987
Tsuguo Naruke1934 – 2006
Naruke map Mountain-DresslerATS map
N1 N2
5th Edition ТNM classification (lung cancer) -1997
6th Edition TNM classification (lung cancer) - 2006
Stage
Occult carcinoma Tх N0 M0
Stage 0 Тis N0 M0
Stage І А T1 N0 M0
Stage І В T2 N0 M0
Stage ІІ А T1 N1 M0
Stage ІІ В T2 N1 M0
T3 N0 M0
Stage ІІІ А T1 N2 M0
T2 N2 M0
T3N1-2 M0
Stage ІІІ В any T N3 M0
Т4 any N M0
Stage ІV any Т any N M1
5319 pts
• 5319 pts North Am; 1975-1988
• Improvement in grouping of ptswith similar prognosis
• Limitations– Selected population of pts
– One geographic region
– No results validation
7th Edition ТNM
lung cancer – 2009
International Staging
Project on Lung Cancer
Peter Goldstraw
International Association for the
Study of Lung Cancer (IASLC)
The IASLC Lung Cancer DatabaseSummary of Cases Contributed to Project (1990 – 2000)
Total cases submitted 100,869
• Excluded from analyses 19,854
• Outside of 1990-2000 time frame 5,443
• Incomplete survival data 1,505
• Unknown histology 2,468
• Incomplete stage information 7,720
• Recurrent cases and other exclusions 1,603
• Carcinoids, sarcomas and other histologies 1,115
Included in analyses 81,015
•Small Cell Lung Cancer (and mixed SCLC/NSCLC) 13,290
•Non-Small Cell Lung Cancer 67,725
Updated from: Goldstraw P, Crowley JJ. The International Association for
the Study of Lung Cancer International staging project on lung cancer. J
Thorac Oncol 2006; 1: 281-286.
• 81495pts fulfilled the inclusion criteria
• 20 countries; Asia, Europe, N.America, Australia
• 45 different databases
Surgical
Series
Clinical
Trial
Surgical
Registry
0
5000
10000
15000
20000
0
2000
4000
6000
8000
10000
12000
Europe Australia N. America Asia
I
II
III
IV
The IASLC Lung Cancer Database
Clinical Stage Distribution by Continent, Non-small Cell Lung Cancer 53,646 Cases
Cancer Research and Biostatistics (CRAB)
Seattle, Washington, USA
• Internally validated by geographic regionand type of database
• Externally validated by being testedagainst the Surveillance, Epidemiology andEnd Results registries
Surgery
36%
Chemotherapy
21%
RT
11%
Surgery + Chemo
4%
Surgery + RT4%
Chemo + RT12%
Surgery + Chemo
+ RT 3%
WHAT’S NEW?
• NSCLC changes– T
• Size• Simultaneous nodule
– N• New LN map
– M• Malignant pleural
effusion
• SCLC staging strategy• Carcinoid tumors• New preoperative
functional assessment
T descriptors
Tumor sze- A 2cm cutpoint subdivides T1a and T1b- A 5cm cutpoint subdivides T2a and T2b
Rami-Porta R et; J Thor Oncol 2007;2:593-602
<2cm = T1a5y sv 77%
2-3cm = T1b5y sv 71%
3-5cm = T2a5y sv 58%
5-7cm = T2b5y sv 49%
>7cm = T35y sv 35%
T1a vs T1b(cut-point 2cm)
T2a vs T2b(cut-point 5cm)
T descriptorsSatelite nodules
The presence of an ipsilateralnodule in a different lobe isnow T4
The presence of satellite nodulesin the same lobe as the primarytumor is now T3
Previously: T4 Previously: M1
N descriptor
• No changes have been madein the N descriptor asdefined in the previous TNMstaging system
• IASLC International StagingCommittee has developed anew node map:
- UPPER ZONE: stations 1 to 4
- AORTOPULMONARY ZONE: stations 5 and 6
- SUBCARINAL ZONE: station 7
- LOWER ZONE: stations 8 and 9
- HILAR ZONE: stations 10 and 11
- PERIPHERAL ZONE: stations 12 to 14
• Survival analysis by the number of involved nodal zones:– Single N1 (48%)– Multiple N1 or single N2 (35%/34%)– Multiple N2 (20%)
Multilevel N2 disease not recommended for primary surgical resection
Sakao Ann Thor Surg 2006
M descriptors
The M descriptor defines the extent of spread to distantsites:
• Mo: No distant metastasis• M1a: Separate tumor nodules in a contralateral lobe or tumor with
pleural nodules or malignant pleural dissemination.• M1b: Distant metastasis
M1a nodule in contralateral lung
Previously: T4
Previously: T4
M1a pleural metastases
M1b distant (extrathoracic) metastases
Previously: M
NB!Paraneoplastic syndrome is not accepted as a metastatic process and is not a contraindication for surgical treatment
- 1950 Veterans Administration Lung Study Group (VALSG)- 1989 IASLC- 2010 IASLC/UICC, 7th edition
histology at initial presentation; adequate staging information atbaseline; adequate follow-up12620 cases
SCLC
VI vs VII Edition
CO-MORBIDITIES
• PE
• Cardiac diseases
• Lung diseases– Emphysema
– COOPD
• Second primary tumor
A Charloux et al; Lung function evaluation before surgery in lung cancer patients: how are recent advances put into practice? A survey among members of the European Society of Thoracic Surgeons (ESTS) and of the Thoracic Oncology Section of the European Respiratory Society (ERS)
• preliminary cardiologic screening
• systematic measurement of the diffusing capacity for carbon monoxide (DLCO)
Decreased performance status was associated with an increased mortality and was shown to be an independent significant factor in determining survival
Conclusions
• The revised staging system – Is more accurately correlated with survival when
compared with the prior staging system
– Is more closely reflected trends in both definitive and paliative treatment
The Future
“Follow up” of the present data basis
8th Edition 2016
Prospective analysis (prognostic information based on the tu
biology and tu genetics; implication of imaging)
9th Edition 2023
All treatment decisions in oncology practice are based on the available
prognostic data
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